Diethylamine → HCID 9951702, compound

HRID 2232514Notes

Reaction equation

HRID 2232514 reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[N:19]=[C:18]([CH2:20][CH2:21][C:22]([OH:24])=O)[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[N:11]=2)=[CH:6][CH:5]=1)([O-:3])=[O:2].C(N1C=CN=C1)(N1C=CN=C1)=O.[CH2:37]([NH:39][CH2:40][CH3:41])[CH3:38]>O1CCCC1>[CH2:37]([N:39]([CH2:40][CH3:41])[C:22](=[O:24])[CH2:21][CH2:20][C:18]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[N:11]=[C:10]([C:7]2[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:9][CH:8]=2)[N:19]=1)[CH3:38]

Participants

5

Procedure

The procedure is as in Example 7, starting with 2-(4-nitrophenyl)-4-quinazolinepropanoic acid (1.35 g), carbonyldiimidazole (0.82 g) and diethylamine (0.9 cc) in anhydrous tetrahydrofuran (20 cc). After chromatography on silica gel with ethyl acetate as eluant, and recrystallization in ethyl acetate, N,N-diethyl-2-(4-nitrophenyl)-4-quinazolinepropanamide (0.35 g), m.p. 168° C., is obtained.

Workup

  1. customAfter chromatography on silica gel with ethyl acetate as eluant, and recrystallization in ethyl acetate

Sources & evidence

ORD record
ord-16d36a9dc1fc404a881be9cdecbfc105
Source dataset
uspto-grants-1988_11
Patent number
US04788199

Reaction notes

Loading…